A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615253



Internal ID16055976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116368348..116409768hg38UCSC Ensembl
Innerchr9:119130627..119172047hg19UCSC Ensembl
Innerchr9:118170448..118211868hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3841421
hg1941421
hg1841421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141282
Samples
Known GenesPAPPA, PAPPA-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615253
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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